A carregar...

Functional consequences of Rett syndrome mutations on human MeCP2

The neurodevelopmental disorder known as Rett syndrome has recently been linked to the methyl-CpG-binding transcriptional repressor, MeCP2. In this report we examine the consequences of these mutations on the function of MeCP2. The ability to bind specifically to methylated DNA and the transcription...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Yusufzai, Timur M., Wolffe, Alan P.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2000
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC113135/
https://ncbi.nlm.nih.gov/pubmed/11058114
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!